Bio-oil Upgrading via High-Pressure Reactive Distillation

This study aims to investigate the roles of process parameters especially pressure and the major components in the high-pressure reactive distillation of bio-oil. The bio-oil distillation fraction yields and properties were evaluated to demonstrate the advantages of the distillation at elevated pressures over distillation at atmospheric pressure. The results indicate that high-pressure distillation can achieve high distillate yields with reduced polymerisation because high pressure can retain water and other light components in the liquid phase

Immersion/Electroless Deposition of Cu on Ta

Continuous Cu films are deposited on Ta by a two-step process; galvanic displacement of Ta by Cu from ammonium fluoride solutions and subsequent electroless Cu deposition from a formaldehyde-containing bath. The conditions necessary for good adhesion are discussed. The extent of oxide film removal in the HF pretreatment solution is studied by electrochemical impedance spectroscopy. The charge-transfer resistance of about 57 Ω-cm2 is several orders of magnitude lower than that measured for the Ta native oxide. These results are consistent with the removal of the Ta2O5 portion of the native oxide

Evolution of magnetic fields and mass flow in a decaying active region

Five days of coordinated observation were carried out from 24–29 September, 1987 at Big Bear and Huairou Solar Observatories. Longitudinal magnetic fields of an αp sunspot active region were observed almost continuously by the two observatories. In addition, vector magnetic fields, photospheric and chromospheric Doppler velocity fields of the active region were also observed at Huairou Solar Observatory. We studied the evolution of magnetic fields and mass motions of the active region and obtained the following results: (1) There are two kinds of Moving Magnetic Features (MMFs). (a) MMFs with the same magnetic polarity as the center sunspot. These MMFs carry net flux from the spot, move through the moat, and accumulate at the moat's outer boundary. (b) MMFs in pairs of mixed polarity. These MMFs are not responsible for the decay of the spot since they do not carry away the net flux. MMFs in category (b) move faster than those of (a). (2) The speed of the mixed polarity MMFs is larger than the outflow measured by photospheric Dopplergrams. The uni-polar MMFs are moving at about the same speed as the Doppler outflow. (3) The chromospheric velocity is in approximately the opposite direction from the photospheric velocity. The photospheric Doppler flow is outward; chromospheric flow is inward. We also found evidence that downward flow appears in the photospheric umbra; in the chromosphere there is an upflow

A comparative study of reduced graphene oxide modified TiO2, ZnO and Ta2O5 in visible light photocatalytic/photochemical oxidation of methylene blue

Reduced graphene oxide (rGO) was applied to prepare various composites of rGO/photocatalyst of G/TiO2, G/ZnO and G/Ta2O5, using titanium (IV) isopropoxide, Zn powder and commercial Ta2O5 powder as photocatalyst precursors, respectively. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric-differential thermal analysis (TG-DTA) and UV–vis diffuse reflectance (UV–vis DRS) were employed to investigate the crystal structure, morphology, surface groups, rGO loading, and optical properties of the produced composites. The photocatalytic activities of the composites under UV–vis and visible light were studied in degradation of methylene blue (MB). G/Ta2O5 showed an enhanced efficiency under UV–vis irradiation. G/TiO2 demonstrated an effective degradation of MB under visible light. The effects of various oxidants, peroxymonosulfate (PMS), peroxydisulfate (PDS) and hydrogen peroxide (H2O2) on MB degradation were thoroughly investigated. H2O2 was a promising oxidant for promoting MB degradation under visible light. The mechanism of the enhanced efficiency in the system of G/TiO2+ vis + H2O2 was discussed

Rational catalyst design for N2 reduction under ambient conditions: Strategies towards enhanced conversion efficiency

Ammonia (NH3), one of the basic chemicals in most fertilizers and a promising carbon-free energy storage carrier, is typically synthesized via the Haber–Bosch process with high energy consumption and massive emission of greenhouse gases. The photo/electrocatalytic nitrogen reduction reaction (NRR) under ambient conditions has attracted increasing interests recently, providing alternative routes to realize green NH3 synthesis. Despite rapid advances achieved in this most attractive research field, the unsatisfactory conversion efficiency including a low NH3 yield rate, and limited Faradaic efficiency or apparent quantum efficiency still remains as a great challenge. The NRR performance is intrinsically related to the electronic and surface structure of catalysts. Rational design and preparation of advanced catalysts are indispensable to improve the performance (e.g., activity and selectivity) of NRR. In this Review, various strategies for the development of desirable catalysts are comprehensively summarized, mainly containing the defect engineering, structural manipulation, crystallographic tailoring, and interface regulation. State-of-the-art heterogeneous NRR catalysts, prevailing theories and underlying catalytic mechanisms, together with current issues, critical challenges, and perspectives are discussed. It is highly expected that this Review will promote the understanding of recent advances in this area and stimulate greater interests for designing promising NRR catalysts in future

Activated carbons as green and effective catalysts for generation of reactive radicals in degradation of aqueous phenol

Several activated carbons (ACs) were used as metal-free catalysts for degradation of a toxic organiccompound, phenol, in the presence of different oxidants, H2O2, peroxydisulfate (PS) and peroxymonosulfate (PMS). It was found that ACs were effective in heterogeneous activation of PMS toproduce sulfate radicals for degradation of phenol, much better than H2O2 and PS. Particle size of AC significantly influenced AC activity, and powder AC was much more effective than granular AC. The complete phenol removal could be achieved in 15 min on powder activated carbon (PAC) under the conditions of [phenol] = 25 mg L-1, [PAC] = 0.2 g L-1, [PMS] = 6.5 mmol L-1, and T = 25 degrees Celcius. It was also found that phenol degradation was significantly influenced by PMS loading, catalyst loading, phenol concentration and temperature. Surface activation of PMS and phenol adsorption played important roles in phenol degradation. Surface coverage by intermediate adsorption and structural change induced deactivation of AC and catalytic activity could be partially recovered by regeneration using calcination

Effects of nitrogen-, boron-, and phosphorus-doping or codoping on metal-free graphene catalysis

Graphene-based materials have been demonstrated as excellent alternatives to traditional metal-based catalysts in environmental remediation. The metal-free nature of the nanocarbons can completely prevent toxic metal leaching and the associated secondary contamination. In this study, nitrogen doped graphene (NG) at a doping level of 6.54 at.% was prepared at mild conditions. Moreover, B- and P-doping or codoping with N in graphene were also achieved by a simple route. The modified graphene can efficiently activate peroxymonosulfate (PMS) to produce sulfate radicals to oxidize phenol solutions. Kinetic studies indicated that initial phenol concentration, PMS dosage, and temperature presented significant influences on the degradation rates. Electron paramagnetic resonance (EPR) analysis provided further insights into the evolution of active radicals during the activation of PMS and SO4•− was believed to be the primary radicals in the oxidation reactions. This study demonstrated a metal-free material for green catalysis in environmental remediation

Co3O4 nanocrystals with predominantly exposed facets: Synthesis, environmental and energy applications

Facet-dependent properties of novel metal or metal-oxide nanocrystals were discovered recently, and are attracting intensive interest owing to their great potential for various practical applications. Co3O4 as an important transition metal oxide shows electronic, magnetic, and redox properties which have found many applications in energy conversion and storage, magnetic separation, sensor devices and catalysis. This review summarizes the most recent research advances in synthesis and applications of nanosized Co3O4 with predominantly exposed facets, with emphasis on the enhanced performances in catalysis and electrochemical properties. The mechanism for improved selectivity and activity was discussed, and a panorama of the correlations between particle shape, crystal plane, surface atom arrangement, and active sites has been drawn. Insightful findings in this scope may be achieved by forthcoming research in theoretical calculations, rational synthesis, and emerging applications. Thus, researchers can manipulate the synthesis at the atomic level resulting in novel applications of the materials in a wide variety of areas